Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.43 (G)
Location

Chromosome 5:148101392 (forward strand) | View in location tab

Co-located

with COSMIC COSM4003383 (A/G), COSM4003382 (A/G) ; HGMD-PUBLIC CM013815

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

This variation has assays on 11 chips - click the plus to show

Variation displays